Medical Device Manufacturer · US , Tulsa , OK

Barkley House, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1990
1
Total
1
Cleared
0
Denied

Barkley House, Inc. has 1 FDA 510(k) cleared medical devices. Based in Tulsa, US.

Historical record: 1 cleared submissions from 1990 to 1990. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Barkley House, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Barkley House, Inc.

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